1677-43-6

Basic information

• Product Name: AURORA KA-3316
• Synonyms: AURORA KA-3316;4-HYDROXY-7-METHYLQUINOLIN-2(1H)-ONE
• CAS NO: 1677-43-6
• Molecular Formula: C₁₀H₉NO₂
• Molecular Weight: 175.18
• Mol File: 1677-43-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: AURORA KA-3316(CAS DataBase Reference)
• NIST Chemistry Reference: AURORA KA-3316(1677-43-6)
• EPA Substance Registry System: AURORA KA-3316(1677-43-6)

Safety Data

• Hazardous Substances Data: 1677-43-6(Hazardous Substances Data)

Usage

General Description

AURORA KA-3316 is a chemical compound used as a corrosion inhibitor in industrial processes. It is a water-based formulation that contains a blend of multifunctional ingredients designed to protect metals from the harmful effects of corrosion. AURORA KA-3316 is specifically formulated to provide effective protection against corrosion in various applications such as industrial water treatment, oil and gas production, and metalworking. It is known for its high performance, versatility, and compatibility with different types of metals, making it a popular choice for corrosion protection in various industrial settings.

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Relevant articles and documents

Microwave prompted multigram synthesis, structural determination, and photo-antiproliferative activity of fluorinated 4-hydroxyquinolinones

3-Unsubstituted 4-hydroxyquinolin-2(1H)-one containing F and CF3 substituent in ring is important pharmacological and synthetic target and basic synthones for a number of antibacterial fluoroquinolones and is promising potent and selective glycine site NMDA receptors. A simple facile one-step microwave enhanced multigram synthesis of such fluorinated quinolones in reasonable purity has been developed in excellent yield (85-94%) in 3-5 min, whereas conventional synthesis required the harsh conditions, long reaction period with use of environmentally unacceptable regents giving the required product in lower yield. The phototoxicity as well as the cytotoxic activities of the title compounds are evaluated against leukemia- and adenocarcinoma-derived cell lines in comparison to the normal human keratinocytes. Structure-activity relationships between the chemical structures and the antimycobacterial, antifungal activity of the evaluated compounds are also discussed.